CRISPR Gene Editing Reverses 'Permanent' Vision Loss in Mice-Offering Hope for Retinitis Pigmentosa Patients
'Three blind mice' can see again after scientists restored vision in breakthrough research that could reverse human retinitis pigmentosa.
'Three blind mice' can see again after scientists restored vision in breakthrough research that could reverse human retinitis pigmentosa.
CRISPR edits the genetic code of the body's own stem cells to treat conditions that arise from defective or mutated genes.
The surgery was declared a success, though it isn't clear whether the patient will be able to see out of his new eye again.
The highly-anticipated two-seater received 2,300 reservations from 57 countries and all 50 states in the US.
The authors recommend this combination of drugs and chemoradiation therapy should be established as the new standard of treatment.
Thanks to a revolutionary gene-editing therapy, this teen no longer needs a monthly blood transfusion in order to survive.
A technique used for finding damage in underwater marine structures may be the most successful breakthrough in breast cancer detection yet.
With modern techniques using a patient's own cells, there is finally a treatment for those with heart failure.
For patients with a deadly skin cancer and few treatment options, a drug to boost their immune systems has left 15% with no sign of cancer 3 years later.
A Polish man who was paralyzed from the chest down following a knife attack can now use a walker after receiving a pioneering transplant treatment using cells from his nose. Movement and sensation are now slowly returning to Darek Fidyka, who described the ability to walk again as "an incredible feeling."
Current methods of diagnosis can only screen for about 19 different kinds of bacteria - this one can quickly and effectively test for 307.
Researchers announced that they have essentially stopped the progression of amyotrophic lateral sclerosis (ALS), or Lou Gehrig's disease, for nearly two years, allowing the mice to approach their normal lifespan. Scientists at Oregon State University say the findings are some of the most compelling ever produced in the search for a therapy to help sufferers […]
Scientists have used a genetically modified herpes virus to cure skin cancer and are looking at another viruses to learn new ways to fight disease.
Three independent studies have now shown that our understanding of the physical makeup of cancer tumors has been based on a myth. A portion of the cells are now seen to be cancer stem cells which are responsible for causing a tumor to grow and develop. Treatments, therefore, can be focused on killing these cells rather than targeting the wider community of tumor cells.
Stanford researchers found an antibody that was found to dramatically shrink or eradicate human cancer tumors that were transplanted into laboratory mice, no matter which type of cancer created the tumor. The research is unique in the variety of solid cancers that responded to the antibody.
Stanford researchers found an antibody that was found to dramatically shrink or eradicate human cancer tumors that were transplanted into laboratory mice, no matter which type of cancer created the tumor. The research is unique in the variety of solid cancers that responded to the antibody.
Instead of experimenting on mice, researchers went straight to testing on human cells – and their studies have been proven successful in halting Alzheimer's in its tracks.
UCSD researchers are gearing up to begin a phase 2 clinical trial for a hydrogel that repairs heart tissue after a successful test in humans proving safety.
When doctors failed to diagnose a young man and his mystery illness, he spent years studying medicine until he finally invented a surgery to save himself.
Not only has Su Metcalfe's treatment succeeded in early trials, it involves zero drugs and no side effects—and it could begin human trials as soon as 2020.
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